Results 161 to 170 of about 4,369 (198)
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Russian Journal of Clinical Dermatology and Venereology, 2023
The clinical case of Muir-Torre syndrome in a patient with multifocal synchronous basal cell skin cancer with sebaceous differentiation and endometrial cancer in a medical history, including clinical manifestations and dermatoscopic pattern features of sebaceous adenoma, epithelioma with sebaceous glandular differentiation and sebaceous glandular skin ...
T.G. Sedova, V.D. Elkin
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The clinical case of Muir-Torre syndrome in a patient with multifocal synchronous basal cell skin cancer with sebaceous differentiation and endometrial cancer in a medical history, including clinical manifestations and dermatoscopic pattern features of sebaceous adenoma, epithelioma with sebaceous glandular differentiation and sebaceous glandular skin ...
T.G. Sedova, V.D. Elkin
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Dermatologic Clinics, 1995
The Muir-Torre syndrome is an autosomal dominantly inherited genodermatosis with malignant potential that is characterized by the presence of at least one sebaceous gland tumor (adenoma, epithelioma, or carcinoma) and a minimum of one internal malignancy. The syndrome has been documented in 147 individuals. Associated features in some of the Muir-Torre
P R, Cohen +3 more
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The Muir-Torre syndrome is an autosomal dominantly inherited genodermatosis with malignant potential that is characterized by the presence of at least one sebaceous gland tumor (adenoma, epithelioma, or carcinoma) and a minimum of one internal malignancy. The syndrome has been documented in 147 individuals. Associated features in some of the Muir-Torre
P R, Cohen +3 more
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Journal of Surgical Oncology, 1986
AbstractThe patient with sebaceous skin tumors and visceral malignancies, Muir‐Torre syndrome, is presented. The documentation of tumors in 8 of 13 members in her kindred supports the concept that this syndrome represents a cancer‐disposing phenotype.
C, Shapiro +4 more
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AbstractThe patient with sebaceous skin tumors and visceral malignancies, Muir‐Torre syndrome, is presented. The documentation of tumors in 8 of 13 members in her kindred supports the concept that this syndrome represents a cancer‐disposing phenotype.
C, Shapiro +4 more
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Journal of the Dermatology Nurses' Association, 2017
ABSTRACT Muir–Torre syndrome is a rare autosomal dominant condition characterized by the development of internal malignancies and sebaceous neoplasms. The most common visceral malignancies associated with the disease are colon cancer, genitourinary cancer, breast cancer, and gastric cancer.
Lacey Roybal, Kim Carlson
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ABSTRACT Muir–Torre syndrome is a rare autosomal dominant condition characterized by the development of internal malignancies and sebaceous neoplasms. The most common visceral malignancies associated with the disease are colon cancer, genitourinary cancer, breast cancer, and gastric cancer.
Lacey Roybal, Kim Carlson
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Skinmed, 2021
A 64-year-old man was referred to our dermatology clinic with a diagnosis of Muir-Torre syndrome (MTS), he had a history of multiple sebaceous carcinomas and sebaceous adenomas removed over the years. The patient has also had visceral cancer and had undergone a colon resection 17 years before to treat colon cancer and was recently diagnosed with ...
A Caresse, Gamret +7 more
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A 64-year-old man was referred to our dermatology clinic with a diagnosis of Muir-Torre syndrome (MTS), he had a history of multiple sebaceous carcinomas and sebaceous adenomas removed over the years. The patient has also had visceral cancer and had undergone a colon resection 17 years before to treat colon cancer and was recently diagnosed with ...
A Caresse, Gamret +7 more
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2010
Muir-Torre syndrome (MTS) is an autosomal dominant genodermatosis that consists of unusual cutaneous sebaceous neoplasm, with or without kerathoacantomas and one or more low-grade visceral malignancies, with or without colonic polyps, in the absence of other predisposing factors.
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Muir-Torre syndrome (MTS) is an autosomal dominant genodermatosis that consists of unusual cutaneous sebaceous neoplasm, with or without kerathoacantomas and one or more low-grade visceral malignancies, with or without colonic polyps, in the absence of other predisposing factors.
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2013
Muir-Torre syndrome (MTS) is a rare, autosomal dominant genodermatosis characterized by sebaceous neoplasms, keratoacanthomas, and visceral malignancies [1, 2]. MTS is a phenotypic subset of hereditary nonpolyposis colorectal cancer (HNPCC) caused by mutations in mismatch repair genes associated with microsatellite instability [3]. Due to the increased
Adam J. Luber, Joshua A. Zeichner
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Muir-Torre syndrome (MTS) is a rare, autosomal dominant genodermatosis characterized by sebaceous neoplasms, keratoacanthomas, and visceral malignancies [1, 2]. MTS is a phenotypic subset of hereditary nonpolyposis colorectal cancer (HNPCC) caused by mutations in mismatch repair genes associated with microsatellite instability [3]. Due to the increased
Adam J. Luber, Joshua A. Zeichner
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Orvosi hetilap, 1999
Muir-Torre syndrome patients have multiple visceral malignancies along with cutaneous sebaceous tumors and keratoacanthomas. We describe a history of a 64-year-old male patient with 13 tumours, who survived 13 years. The initial ascending colon adenocarcinoma was followed by some different tumors of the skin: adenoma and carcinoma of sebaceous glands ...
L, Tiszlavicz, Z, Hódi, Z, Tihanyi
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Muir-Torre syndrome patients have multiple visceral malignancies along with cutaneous sebaceous tumors and keratoacanthomas. We describe a history of a 64-year-old male patient with 13 tumours, who survived 13 years. The initial ascending colon adenocarcinoma was followed by some different tumors of the skin: adenoma and carcinoma of sebaceous glands ...
L, Tiszlavicz, Z, Hódi, Z, Tihanyi
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Neuromalignancy complicating the Muir–Torre syndrome
Journal of Cutaneous Pathology, 2015Keywords: brain cancer; hereditary nonpolyposis colorectal cancer; immunohistochemistry; Muir–Torre syndrome; sebaceous ...
Drew J B, Kurtzman +3 more
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Muir-Torre Syndrome: A Case Report
Tumori Journal, 1991The authors present a case of Muir-Torre syndrome, the « sporadic » form, with a review of the literature. The importance of the close scrutiny of these patients and their relatives is stressed.
M, Bisceglia, P, Zenarola
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